Evidence map›Paper›PMID 33514835›Full record

ArticleCommunications biology2021

Plexin-B2 facilitates glioblastoma infiltration by modulating cell biomechanics.

Yong Huang, Rut Tejero, Vivian K Lee, Concetta Brusco, Theodore Hannah, Taylor B Bertucci, Chrystian Junqueira Alves, Igor Katsyv, Michael Kluge, Ramsey Foty and 5 more

Open access · goldAbstract readVideo-Audio Media
In one paragraph

Article in Communications biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.2field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 35 citations in OpenAlex.

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  16. Biallelic variants in Plexin B2 (Journal of medical genetics · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 5 institutions in 2 countries.

Yong Huang *Friedman Brain Institute, Nash Family Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID 0000-0001-8095-4215
Rut Tejero *Friedman Brain Institute, Nash Family Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Vivian K LeeDepartment of Bioengineering, Northeastern University, Boston, MA, USA.
Concetta BruscoFriedman Brain Institute, Nash Family Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID 0000-0002-8600-5333
Theodore HannahFriedman Brain Institute, Nash Family Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Taylor B BertucciDepartment of Bioengineering, Northeastern University, Boston, MA, USA.
Chrystian Junqueira AlvesFriedman Brain Institute, Nash Family Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID 0000-0003-2224-0729
Igor KatsyvDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Michael KlugeInstitut für Informatik, Ludwig-Maximilians-Universität München, Munich, Germany.
Ramsey FotyDepartment of Surgery, Robert Wood Johnson Medical School, Rutgers University, New Brunswick, NJ, USA.
Bin ZhangDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Caroline C FriedelInstitut für Informatik, Ludwig-Maximilians-Universität München, Munich, Germany.ORCID 0000-0003-3569-4877
Guohao DaiDepartment of Bioengineering, Northeastern University, Boston, MA, USA.
Hongyan ZouFriedman Brain Institute, Nash Family Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY, USA. hongyan.zou@mssm.edu.ORCID 0000-0003-4216-5607
Roland H FriedelFriedman Brain Institute, Nash Family Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY, USA. roland.friedel@mssm.edu.ORCID 0000-0002-7513-3604
Allen Institute for Brain Science · USNortheastern University · USIcahn School of Medicine at Mount Sinai · USLudwig-Maximilians-Universität München · DERutgers, The State University of New Jersey · US

Funding

THE TISCH CANCER INSTITUTE - CANCER CENTER SUPPORT GRANTP30CA196521 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Ramon E Parsons · 2015 to 2026
$35.4M
Plexin-B2 function in glioma invasion and glioma stem cell maintenanceR01NS092735 · NINDS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI FRIEDEL, ROLAND HORST · 2016 to 2025
$4.1M
Dissect governing factors for tumor stem cell dormancy in biomimetic vascular/GBM modelR01NS107462 · NINDS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI DAI, GUOHAO, FRIEDEL, ROLAND HORST · 2018 to 2022
$3.0M
NCI NIH HHS P30 CA196521NINDS NIH HHS R01 NS092735NINDS NIH HHS R01 NS107462
6 · The paper itself

Abstract

Infiltrative growth is a major cause of high lethality of malignant brain tumors such as glioblastoma (GBM). We show here that GBM cells upregulate guidance receptor Plexin-B2 to gain invasiveness. Deletion of Plexin-B2 in GBM stem cells limited tumor spread and shifted invasion paths from axon fiber tracts to perivascular routes. On a cellular level, Plexin-B2 adjusts cell adhesiveness, migratory responses to different matrix stiffness, and actomyosin dynamics, thus empowering GBM cells to leave stiff tumor bulk and infiltrate softer brain parenchyma. Correspondingly, gene signatures affected by Plexin-B2 were associated with locomotor regulation, matrix interactions, and cellular biomechanics. On a molecular level, the intracellular Ras-GAP domain contributed to Plexin-B2 function, while the signaling relationship with downstream effectors Rap1/2 appeared variable between GBM stem cell lines, reflecting intertumoral heterogeneity. Our studies establish Plexin-B2 as a modulator of cell biomechanics that is usurped by GBM cells to gain invasiveness.

Indexed as

Cell MovementAdaptor Proteins, Signal TransducingAnimalsBiomechanical PhenomenaBrain NeoplasmsCell Line, TumorCell-Matrix JunctionsGene Expression Regulation, NeoplasticGlioblastomaHumansMaleMiceMice, Inbred ICRMice, SCIDNeoplasm InvasivenessNerve Tissue ProteinsAdaptor Proteins, Signal TransducingNerve Tissue ProteinsPLXNB2 protein, humanRAP2A protein, humanrap GTP-Binding ProteinsSema4c protein, humansemaphorin 4B, humanSemaphorinsShelterin ComplexTelomere-Binding ProteinsTERF2IP protein, humanTranscription FactorsYAP1 protein, humanYAP-Signaling Proteins

Identifiers

PMID33514835
PMCPMC7846610
OpenAlexW3125937539

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.